# FDA Inspection 1096129 - Ray America Inc - April 15, 2019

Source: https://www.keypedia.com/records/fda_inspections/ray-america-inc/71d21ba1-104d-4f5f-96c4-62ac4e2c6d2b
Source feed: FDA_Inspections

> FDA Inspection 1096129 for Ray America Inc on April 15, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1096129
- Company Name: Ray America Inc
- Inspection Date: 2019-04-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1096129 - 2019-04-15](https://www.keypedia.com/records/fda_inspections/ray-america-inc/15594f0c-cd67-461f-8609-efa7a30835b3)
- [FDA Inspection 1096129 - 2019-04-15](https://www.keypedia.com/records/fda_inspections/ray-america-inc/0e806f22-9119-4de6-85f5-74454a6804eb)

Company: https://www.keypedia.com/companies/ray-america-inc/9a380e18-27a9-4af8-af3c-a2f01aa6ee46

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7